| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Epileptic encephalopathy +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene